Eric Engel
Impact in
- Genetics top 1%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
-
- Prenatal Screening and Diagnostics
Papers in ⓘ
- Genetics 51
- Genomic variations and chromosomal abnormalities 18
- Genetic Syndromes and Imprinting 12
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 10
- Co-authors
- Anne P. Forbes (3 shared papers)C.D. DeLozier-Blanchet (6 shared papers)Walter E. Nance (7 shared papers)E. D. Williams (1 shared paper)Celia D. Delozier (4 shared papers)Suzanne B. Cassidy (5 shared papers)L. Clifford McKee (2 shared papers)John M. Flexner (2 shared papers)
- Journals
- The Lancet (11 papers)Cytogenetic and Genome Research (5 papers)New England Journal of Medicine (4 papers)The Journal of Pediatrics (3 papers)Journal of Cell Science (3 papers)
- Partner nations
- United StatesSwitzerlandUnited Kingdom
In The Last Decade
Eric Engel
97 papers receiving 2.4k citations
Hit Papers
Peers
Comparison fields: 5 of 111
- Genetics 1.8k
- Pediatrics, Perinatology and Child Health 922
- Developmental Biology 92
- Genetics 178
- Molecular Biology 1.1k
Countries citing papers authored by Eric Engel
This map shows the geographic impact of Eric Engel's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Eric Engel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eric Engel more than expected).
Fields of papers citing papers by Eric Engel
This network shows the impact of papers produced by Eric Engel. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Eric Engel. The network helps show where Eric Engel may publish in the future.
Co-authors
The 25 scholars most cited alongside Eric Engel, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 99 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A new genetic concept: Uniparental disomy and its potential effect, isodisomy Hit paper breakdown → | 1980 | 408 |
| 2 | 1995 | 277 | |
| 3 | 1965 | 106 | |
| 4 | 1991 | 103 | |
| 5 | 1964 | 101 | |
| 6 | 2006 | 99 | |
| 7 | 1994 | 99 | |
| 8 | 1963 | 94 | |
| 9 | Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21. | 1992 | 86 |
| 10 | 1993 | 72 | |
| 11 | 1966 | 47 | |
| 12 | 1982 | 46 | |
| 13 | 1987 | 44 | |
| 14 | 1974 | 40 | |
| 15 | 1967 | 36 | |
| 16 | 1980 | 36 | |
| 17 | 1966 | 35 | |
| 18 | 1969 | 35 | |
| 19 | 1969 | 31 | |
| 20 | 1961 | 30 |
About Eric Engel
Eric Engel is a scholar working on Genetics, Developmental Biology, Pediatrics, Perinatology and Child Health, Hematology and Anatomy, having authored 99 papers that have together received 2.6k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (21 papers), Genomic variations and chromosomal abnormalities (18 papers), Genetic Syndromes and Imprinting (12 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers), Sexual Differentiation and Disorders (9 papers), Chromosomal and Genetic Variations (8 papers), Acute Myeloid Leukemia Research (7 papers) and Chronic Myeloid Leukemia Treatments (6 papers). The work is most often cited by research in Genetics (1.8k citations), Pediatrics, Perinatology and Child Health (922 citations), Developmental Biology (92 citations), Genetics (178 citations) and Molecular Biology (1.1k citations). Eric Engel has collaborated with scholars based in United States, Switzerland and United Kingdom. Frequent co-authors include Anne P. Forbes, C.D. DeLozier-Blanchet, Walter E. Nance, E. D. Williams, Celia D. Delozier, Suzanne B. Cassidy, L. Clifford McKee, John M. Flexner, Christiane Werner‐Favre and Jan van Eys. Their work appears in journals such as The Lancet, Cytogenetic and Genome Research, New England Journal of Medicine, The Journal of Pediatrics and Journal of Cell Science.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.